About: Major molecular response achieved with dasatinib in a CML patient with F317L BCR-ABL kinase domain mutation     Goto   Sponge   NotDistinct   Permalink

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Description
  • Mutations of BCR-ABL tyrosine kinase domain represent the most frequently identified and best-studied mechanism of chronic myeloid leukemia (CML) resistance to the treatment with tyrosine kinase inhibitors (TKIs). In previously reported patients with F317L BCR-ABL kinasedomain mutation response to dasatinib treatment was invariably poor. We describe a CML patient in chronic phase with F317L mutation identified shortly after the initiation of dasatinib therapy,following previous imatinib failure. Despite a continual persistence of the F317L mutation, thepatient achieved a complete cytogenetic and a major molecular response after 4 and 6 months of dasatinib treatment, respectively, and maintained the response for more than 20 months of followup.Possible explanations for this long-term favourable response may include immune-mediatedeffects associated with dasatinib therapy, elimination of proliferative advantage of F317L-mutant cells through inhibition of Src family of kinases (SFK) or the presence of F3
  • Mutations of BCR-ABL tyrosine kinase domain represent the most frequently identified and best-studied mechanism of chronic myeloid leukemia (CML) resistance to the treatment with tyrosine kinase inhibitors (TKIs). In previously reported patients with F317L BCR-ABL kinasedomain mutation response to dasatinib treatment was invariably poor. We describe a CML patient in chronic phase with F317L mutation identified shortly after the initiation of dasatinib therapy,following previous imatinib failure. Despite a continual persistence of the F317L mutation, thepatient achieved a complete cytogenetic and a major molecular response after 4 and 6 months of dasatinib treatment, respectively, and maintained the response for more than 20 months of followup.Possible explanations for this long-term favourable response may include immune-mediatedeffects associated with dasatinib therapy, elimination of proliferative advantage of F317L-mutant cells through inhibition of Src family of kinases (SFK) or the presence of F3 (en)
Title
  • Major molecular response achieved with dasatinib in a CML patient with F317L BCR-ABL kinase domain mutation
  • Major molecular response achieved with dasatinib in a CML patient with F317L BCR-ABL kinase domain mutation (en)
skos:prefLabel
  • Major molecular response achieved with dasatinib in a CML patient with F317L BCR-ABL kinase domain mutation
  • Major molecular response achieved with dasatinib in a CML patient with F317L BCR-ABL kinase domain mutation (en)
skos:notation
  • RIV/61989592:15110/09:00009742!RIV10-MSM-15110___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(NS9949), Z(MSM6198959205), Z(MSM6198959223)
http://linked.open...iv/cisloPeriodika
  • 4
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 324437
http://linked.open...ai/riv/idVysledku
  • RIV/61989592:15110/09:00009742
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • chronic myeloid leukemia; F317L BCR-ABL mutation; dasatinib; tyrosine kinase inhibitors (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [9F7C47E59E16]
http://linked.open...i/riv/nazevZdroje
  • Leukemia Research
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 34
http://linked.open...iv/tvurceVysledku
  • Faber, Edgar
  • Indrák, Karel
  • Jarošová, Marie
  • Divoká, Martina
  • Rožmanová, Šárka
  • Mojzíková, Renáta
  • Plachý, Radek
  • Šťastný, Marek
http://linked.open...n/vavai/riv/zamer
issn
  • 0145-2126
number of pages
http://localhost/t...ganizacniJednotka
  • 15110
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